Predicted Trait | |
Reported Trait | Coronary heart disease |
Mapped Trait(s) | coronary artery disease (EFO_0001645) |
Score Construction | |
PGS Name | INTERVENE_MegaPRS_CHD |
Development Method | |
Name | megaprs.auto |
Parameters | BayesR, p1=0.89, p2=0.05, p3= 0.05, p4=0.01 |
Variants | |
Original Genome Build | GRCh37 |
Number of Variants | 610,677 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000618 |
Citation (link to publication) | Jermy B et al. Nat Commun (2024) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | |
Score Development/Training | European: 100% 404 individuals (100%) |
PGS Evaluation | European: 100% 7 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST004787 Europe PMC: 28714975 |
63,731 individuals | European, NR | NR |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) | Phenotype Definitions & Methods | Age of Study Participants | Participant Follow-up Time | Additional Ancestry Description | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
— | 404 individuals | European | 1000G | — | — | — | non-Finnish Europeans | — |
PGS Performance Metric ID (PPM) |
PGS Sample Set ID (PSS) |
Performance Source | Trait |
PGS Effect Sizes (per SD change) |
Classification Metrics | Other Metrics | Covariates Included in the Model |
PGS Performance: Other Relevant Information |
---|---|---|---|---|---|---|---|---|
PPM021209 | PSS011573| European Ancestry| 38,448 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.18 [1.16, 1.2] | C-index: 0.55 [0.55, 0.56] | — | PCs 1-10 | — |
PPM021210 | PSS011572| European Ancestry| 69,715 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.39 [1.36, 1.42] | C-index: 0.6 [0.59, 0.6] | — | PCs 1-10 | — |
PPM021211 | PSS011571| European Ancestry| 29,427 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.32 [1.27, 1.38] | C-index: 0.6 [0.58, 0.61] | — | PCs 1-10 | — |
PPM021212 | PSS011569| European Ancestry| 44,168 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.27 [1.23, 1.32] | — | — | PCs 1-10 | — |
PPM021213 | PSS011570| European Ancestry| 7,018 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.13 [1.07, 1.19] | C-index: 0.56 [0.54, 0.57] | — | PCs 1-10 | — |
PPM021214 | PSS011568| European Ancestry| 412,090 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.41 [1.4, 1.43] | C-index: 0.62 [0.62, 0.62] | — | PCs 1-10 | — |
PPM021215 | PSS011567| European Ancestry| 148,312 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident CHD | HR: 1.18 [1.16, 1.21] | C-index: 0.58 [0.57, 0.58] | — | PCs 1-10 | — |
PGS Sample Set ID (PSS) |
Phenotype Definitions and Methods | Participant Follow-up Time | Sample Numbers | Age of Study Participants | Sample Ancestry | Additional Ancestry Description | Cohort(s) | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
PSS011567 | — | — | [
|
— | European | — | EB | — |
PSS011568 | — | — | [
|
— | European | — | FinnGen | — |
PSS011569 | — | — | [
|
— | European | — | G&H | — |
PSS011570 | — | — | [
|
— | European | — | GS:SFHS | — |
PSS011571 | — | — | [
|
— | European | — | GEL | — |
PSS011572 | — | — | [
|
— | European | — | HUNT | — |
PSS011573 | — | — | [
|
— | European | — | MGBB | — |